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Recent Advances in Enantioselective Photochemical Reactions of Stabilized Diazo Compounds

Diazo compounds have proven to be a useful class of carbenes or metal carbenoids sources under thermal, photochemical, or metal-catalyzed conditions, which can subsequently undergo a wide range of synthetically important transformations. Recently, asymmetric photocatalysis has provoked increasing re...

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Detalles Bibliográficos
Autores principales: Hua, Ting-Bi, Yang, Qing-Qing, Zou, You-Quan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749315/
https://www.ncbi.nlm.nih.gov/pubmed/31480796
http://dx.doi.org/10.3390/molecules24173191
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author Hua, Ting-Bi
Yang, Qing-Qing
Zou, You-Quan
author_facet Hua, Ting-Bi
Yang, Qing-Qing
Zou, You-Quan
author_sort Hua, Ting-Bi
collection PubMed
description Diazo compounds have proven to be a useful class of carbenes or metal carbenoids sources under thermal, photochemical, or metal-catalyzed conditions, which can subsequently undergo a wide range of synthetically important transformations. Recently, asymmetric photocatalysis has provoked increasing research interests, and great advances have been made in this discipline towards the synthesis of optically enriched compounds. In this context, the past two decades have been the most productive period in the developments of enantioselective photochemical reactions of diazo compounds due to a better understanding of the reactivities of diazo compounds and the emergence of new catalytic modes, as well as easier access to and treatment of stabilized diazo compounds. This review highlights these impressive achievements according to the reaction type, and the general mechanisms and stereochemical inductions are briefly discussed as well.
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spelling pubmed-67493152019-09-27 Recent Advances in Enantioselective Photochemical Reactions of Stabilized Diazo Compounds Hua, Ting-Bi Yang, Qing-Qing Zou, You-Quan Molecules Review Diazo compounds have proven to be a useful class of carbenes or metal carbenoids sources under thermal, photochemical, or metal-catalyzed conditions, which can subsequently undergo a wide range of synthetically important transformations. Recently, asymmetric photocatalysis has provoked increasing research interests, and great advances have been made in this discipline towards the synthesis of optically enriched compounds. In this context, the past two decades have been the most productive period in the developments of enantioselective photochemical reactions of diazo compounds due to a better understanding of the reactivities of diazo compounds and the emergence of new catalytic modes, as well as easier access to and treatment of stabilized diazo compounds. This review highlights these impressive achievements according to the reaction type, and the general mechanisms and stereochemical inductions are briefly discussed as well. MDPI 2019-09-02 /pmc/articles/PMC6749315/ /pubmed/31480796 http://dx.doi.org/10.3390/molecules24173191 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hua, Ting-Bi
Yang, Qing-Qing
Zou, You-Quan
Recent Advances in Enantioselective Photochemical Reactions of Stabilized Diazo Compounds
title Recent Advances in Enantioselective Photochemical Reactions of Stabilized Diazo Compounds
title_full Recent Advances in Enantioselective Photochemical Reactions of Stabilized Diazo Compounds
title_fullStr Recent Advances in Enantioselective Photochemical Reactions of Stabilized Diazo Compounds
title_full_unstemmed Recent Advances in Enantioselective Photochemical Reactions of Stabilized Diazo Compounds
title_short Recent Advances in Enantioselective Photochemical Reactions of Stabilized Diazo Compounds
title_sort recent advances in enantioselective photochemical reactions of stabilized diazo compounds
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749315/
https://www.ncbi.nlm.nih.gov/pubmed/31480796
http://dx.doi.org/10.3390/molecules24173191
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